Daig Corp.
Mchenry, IL, US
Daig Corp. appears in FDA device records in Mchenry, IL. FDA records list 27 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 27
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 27 510(k) clearances for Daig Corp. between 1977 and 1983. The busiest year on record is 1980, with 11. The most recent is 1983, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1977 | 6 |
| 1978 | 3 |
| 1979 | 2 |
| 1980 | 11 |
| 1981 | 3 |
| 1983 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K830743 | POROUS TIP ENDOCARDIAL LEAD | DTB | Substantially Equivalent | |
| K830464 | PACEMAKER ELECTRODE PERM. & TEMP | DTB | Substantially Equivalent | |
| K802553 | PERM. ENDOCARDIAL UNIPOLAR WEDGE URETHAN | DTB | Substantially Equivalent | |
| K802552 | PERM. ENDOCARDIAL UNIPOLAR TINED/WEDGE | DTB | Substantially Equivalent | |
| K802547 | PERMANENT & TEMP. PACEMAKER ELECTRODE | DTB | Substantially Equivalent | |
| K800795 | PERMANENT & TEMP. PACEMAKER ELECTRODE | DTB | Substantially Equivalent | |
| K800354 | LEAD, TINED PACING, IMPLANTABLE | DTB | Substantially Equivalent | |
| K800356 | PERMANENT LEAD INTRADUCER | DYB | Substantially Equivalent | |
| K800355 | LEAD, SUTURELESS MYOCARDIAL | DTB | Substantially Equivalent | |
| K800353 | ADAPTER KIT | DTD | Substantially Equivalent | |
| K800352 | PACEMAKER, ELECTRODE | DTB | Substantially Equivalent | |
| K800351 | PACEMAKER, ELECTRODE, PERM. & TEMP. | DTB | Substantially Equivalent | |
| K800350 | ENDOCARD. PACING LEAD STD. LENGTH PL202 | DTB | Substantially Equivalent | |
| K800348 | UNIPOLAR LEAD CONFIGURATION CONDUCTOR | DTB | Substantially Equivalent | |
| K800347 | PERM. INPLANT ENDOCARD. PAC. LEAD | DTB | Substantially Equivalent | |
| K801064 | DISPOSABLE PATIENT CABLE MODEL 5807 | DSA | Substantially Equivalent | |
| K791129 | PERMANENT LEAD INTRADUCER | DYB | Substantially Equivalent | |
| K782087 | LEAD, SUTURELESS MYOCARDIAL | DTB | Substantially Equivalent | |
| K782004 | LEAD, TIMED PACING, IMPLANTABLE | DTB | Substantially Equivalent | |
| K780246 | PACEMAKER, ELECTRODE, PERMANENT & TEMP. | DTB | Substantially Equivalent | |
| K772197 | PACEMAKER, PERM. & TEMP., ELECTRODE | DTB | Substantially Equivalent | |
| K771567 | ENDOCARD. PACING LEAD-LONG LENGTH PL203 | DTB | Substantially Equivalent | |
| K771566 | ENDOCAR. PACING LEAD-STD. LENGTH PL202 | DTB | Substantially Equivalent | |
| K771565 | ENDOCARD. PACIN/ LEAD-LONG LENGTH PL200 | DTB | Substantially Equivalent | |
| K771564 | ENDOCARD. PACIN/ LEAD-STD. LENGTH PL100 | DTB | Substantially Equivalent | |
| K770468 | UNIPOLAR LEAD CONFIGURATION CONDUCTOR | DTB | Substantially Equivalent | |
| K770195 | PERM. IMPLANT. ENDOCARDIAL PAC. LEAD | DTB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Daig Corp. edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
The self-serve claim needs an FDA establishment registration, FEI or owner-operator number on the company’s record, and we hold none for Daig Corp.. The only route for a company with no identifier on record is a person here: write to us, and one looks at the record and sends the same claim link by hand.
Data as of , FDA export datePage updated Source: openFDA, public domain
